(Lepidoptera: Noctuidae) in Puerto Rico

(Lepidoptera: Noctuidae) in Puerto Rico

Life: The Excitement of Biology 3(1) 15 On the Male and Female Genital Structures of Phyllobius (Metaphyllobius) glaucus (Scopoli, 1763) (Coleoptera: Curculionidae: Phyllobinii) from Turkey1 Mahmut Erbey2, Üzeyir Çağlar3, and Selami Candan3 Abstract: Several structures of the male genitalia (tegmen, parameres, manubrium, endophallus), and ninth abdominal sternite (spiculum gastrale) as well as the female genitalia (genital spicule and eight sternite, ovipositor, and spermatheca) of Phyllobius (Metaphyllobius) glaucus are described and illustrated for the first time as they are useful for separating P. glaucus from other congenerics. Key Words: Coleoptera, Curculionidae, Phyllobius glaucus, male and female genitalia Species of the polyphagous weevil genus Phyllobius generally live on cultivated shrubs and trees, particularly those in the families Urticaceae, Betulaceae, Salicaceae, and Rosaceae (Pesarini 1980). Their larvae often feed on the roots and, upon reaching adulthood, the beetles are seen on the shoots (Dieckmann 1980, Ross 1963). Sometimes, both larvae and adults cause major economic damage, particularly when grazing on young plants. Phyllobius (Metaphyllobius) glaucus (Scopoli, 1763) thrives from plains to mountainous and even subalpine zones (Dieckmann 1980). Figure 1. Phyllobius glaucus. Photo copyright 2005 J .K. Lindsey, http://www.commanster.eu. Used with permission. 1 Submitted on February 11, 2015. Accepted on February 21, 2015. Last revisions received on March9, 2015. 2 Department of Biology, Faculty of Art and Science, Ahi Evran University, Kırşehir, Turkey. E- mail: [email protected] . Corresponding Author. 3 Department of Biology, Faculty of Science, Gazi University, Ankara, Turkey. E-mail: [email protected] , [email protected] , respectively. DOI:10.9784/LEB3(1)Erbey.01 Electronically available on April 18, 2015. Mailed on April 18, 2015. Life: The Excitement of Biology 3(1) 16 Structures used in copulation (Figure 2) and reproduction have widespread use for insect identification (Hoffmann 1950, 1954; Tuxen 1970; Pajni et al. 1977; Ter-Minasyan 1978; Pesarini 1980; Caldara 1985, 1990; Sert and Çağatay 1999; Sert 1997, 2006; Yunakov and Korotyaev 2007). The genitalia of Phyllobius (Metaphyllobius) glaucus has been partially illustrated by several authors (Angelov 1976, Pesarini 1980, Yunakov and Korotyaev 2007) although some structures, such as the tegmen, parameres, manubrium, endophallus, ninth abdominal sternite, and the female genitalia remain undescribed, as far as we know. Herein, we describe and illustrate those structures for the first time as they are useful for separating P. glaucus from other congenerics (Figures 3and 4). Figure 2. Mating Phyllobius glaucus (Scopoli, 1763); female to the left, male to the right. Photo taken by Andreas Haselböck (www.naturspaziergang.de). Used with permission. Methods Phyllobius glaucus beetles were collected on meadows from different localities of Yozgat Province (Central Anatolia of Turkey) in 2011. The specimens are deposited at the Ahi Evran University Zoology Museum Entomology (AUZM-Ent.). Identification was made based using the relevant literature (Angelov 1976, Dieckmann 1980, Hoffmann 1950, Pesarini 1980). Male and female genitalia were dissected following standard methods (Erbey and Candan 2010, Erbey et al. 2013). Observations were made using a stereomicroscope (Olympus SZX12 Photomicroscope at 40X). The classification proposed by Alonso-Zarazaga and Lyal (1999) is followed. Nomenclature follows Pajni et al. (1977), Sert (1998, 2006), Tuxen (1970), and Wanat (2007). Life: The Excitement of Biology 3(1) 17 Results Male genitalia: Lateral view. Aedeagal tube curved medially, narrowing towards base; tegmen with parameres located at base of aedeagal tube; manubrium long and curved apically; aedeagal apodemes long and thin, widened basally; aedeagal apodemes clearly curved basally, endophallus spinose, as in Figure 3A. Dorsal view: aedegal tube straight, narrowed apically, apex with a medial suture; tegmen and parameres resemble scissors; aedegal tube strongly sclerotized laterally, medial is transparent; aedegal apodemes distinct; endophallus expanded with strongly sclerotized spines (Figure 3B); ninth abdominal sternite long and thin, basally curved, with an apical fork-like projection, connecting to symmetrical crescent-shaped sclerites by a transparent membrane (Figure 3C). Figure 3. Male genitalia of Phyllobius (Metaphyllobius) glaucus. A. Aedeagus (lateral view): Ae, Aedeagal tube; Aa, Aedeagal apodemes; E, Endophallus; Ma: Manibrium; Tg,Tegmen; Pm, Parameres. B. Aedeagus (dorsal view): Tg, Tegmen; Pm, Parameres. C. Nith abdominal sternite, S9, Sc: Eigth sternite. Female genitalia: Genital spicule and eigth abdominal sternite as in Figure 4A. Genital spicule long and thin, less curved than in conspecific male, connected to a “V” shaped eigth abdominal sternite through a membrane; eigth abdominal sternite with long setae like “V” shape (Figure 4A); ovipositor tubular, translucid, membranous, sides membrane corrugated, apically divided into two, heavily sclerotized coxites (hemisternites) bearing long hairs (Figure 4B); spermatheca hook-like, cornu short, less narrowed apically, proximal bar short and thick, ramus is short, nodul long and distinctly curved apically, narrower than the other parts (Figure 4C). Life: The Excitement of Biology 3(1) 18 Figure 4. Female genitalia of Phyllobius (Metaphyllobius) glaucus female. A. Genital spicule (GS) and eigth abdominal sternite (As). B. Ovipositor: Cox., Coxite (Hemisternite). C. Spermatheca: Cor, Cornu; PA, Proximal bar; R, Ramus; N, Nodul. Discussion Several authors use only the spermatheca for species identification but Pajni et al. (1977) and Sert (1997, 1998, 2000, 2006, 2007) have found that the genital spicule, eigth abdominal sternite, and ovipositor are useful to distinguish species of weevils. Additionally, the shape of the ninth sternite (spiculum gastrale) has been used in identification of some weevils (Clark 1990). The tegmen of P. glaucus, with its parameres and a manubrium, has a unique construction as compared to other species of Phyllobius as is true of the aedeagal apodemes and the spinose endophallus. Angelov (1976), Pesarini (1980), as well as Yunakov and Korotyaev (2007) have illustrated the aedeagal apex (dorsal and ventral) in Phyllobius. We think that systematically illustrating the tegmen, parameres, manibrium, spermatheca, genital spicule, eigth abdominal sternite, and ovipositor should be useful to students of the phylogeny of weevils. Acknowledgments We thank four anonymous reviewers for their constructive suggestions to improve this paper. J. K. Lindley and Andreas Haselböck allowed us to reproduce Figures 1 and 2, respectively. Literature Cited Alonso-Zarazaga, M. A. and Ch. H. C. Lyal. 1999. A World Catalogue of Families and Genera of Curculionoidae (Insecta: Coleoptera) (excepting Scolytidae and Platypodidae). Barcelona, Spain. Entomopraxis 315 pp. Angelov, P. 1976. Fauna Bulgarica 5. Coleoptera, Curculionidae. Part I (Apioninae, Otiorhynchinae). Eadibus Academiae Scientiarum Bulgaricae. Sofya, Bulgaria. 356 pp. Caldara, R. 1985. Revisione delle Sibinia Paleartiche (Coleoptera: Curculionidae). Memorie della Societa Entomologica Italiana 63:24-105. Life: The Excitement of Biology 3(1) 19 Caldara, R. 1990. Revisione Taxonomica delle specie Paleartiche del genere Tychius Germar (Coleoptera, Curculionidae). Memorie della Società Italiana di Scienze Naturali e del Museo Civico di Storia Naturale di Milano 25:53-218. Clark, W. E. 1990. Revision of the flavirostris species group of the genus Anthonomus Germar (Coleoptera: Curculionidae). Transactions of the American Entomological Society 116:261- 294. Dieckmann, L. 1980. Beitrage zur insektenfauna der DDR: Coleoptera-Curculionidae (Brachycerinae, Otiorrhynchinae, Brachyderinae). Beitrage zur Entomology (Berlin, Germany) 30:145-310. Hoffmann, A. 1950. Fauna de France, Coleopteres Curculionides. Premiere Partie 52. Ouvrage Pblie avec le concours du Centre National de la Recherche Scientifique. Paris, France. pp. 1- 486. Hoffmann, A. 1954. Fauna de France, Coleopteres Curculionides. Deuxieme Partie 59. Ouvrage Pblie avec le concours du Centre National de la Recherche Scientifique. Paris, France. pp. 487-1208. Pajni, H. R., S. K. Singal, and B. R. Bhateja. 1977. A study of female genitalia in the families Curculionidae, Brentidaeand Attelabidae (Coleoptera: Curculionidae). Research Bulletin Panjab University 28:69-83. Pesarini, C. 1980. Le specie paleartiche occidentali della tribu Phyllobiini (Coleoptera: Curculionidae). Bulletion Zoologia Agraria Bachicolture 15:49-230. Ross, A. H. 1963. The beetles of the United States. The Catholic University of America. Washington, District of Columbia, USA. 1112 pp. Sert, O. 1997. Investigations on the female genital organ structure in Cleoninae (Coleoptera). Turkish Journal of Entomology 21:147-159. Sert, O. 1998. Studies on the structures of the female genital organs from subfamily Ceutorhynnhinae (Coleoptera: Curculionidae). Turkish Journal of Entomology 22:73-80. Sert, O. 2000. Studies on the structure of the female genital organ of some species from genera Tychius Germar and Sibinia Germar from subfamily Tychiinae, Pachytychius Jekel from subfamily Erirhinae (Coleoptera: Curculionidae). Turkish Journal of Entomology 24:195-203. Sert, O. 2006. On the female and male genital structures of Sitona fairmairei Allard, 1869 (Coleoptera: Curculionidae) fromTurkey. Entomological News 117:441-443.

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